94199-7LOINC 2.82
FGA gene full mutation analysis in Blood or Tissue by Sequencing
FGA Full Mut Anl Bld/T Seq
Definition
- Full gene sequence analysis is performed to test for the presence of a mutation in the coding regions and intron/exon boundaries of the fibrinogen alpha chain (FGA) gene. Mutations in the FGA gene are associated with congenital afibrinogenemia (also hypofibrinogenemia, dysfibrinogenemia, or hypodysfibrinogenemia) and familial renal amyloidosis.[GHR gene: FGA]
Component
- FGA gene full mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH
Property
- Find
Scale
- Doc
Method
- Sequencing
Related names
- Blood; Document; Fib2; fibrinogen alpha chain; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; Molecular pathology; MOLPATH; Mut; Mutations; Next generation sequencing; NGS; Point in time; Random; sequencing of entire coding region; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- Document
- Fib2
- fibrinogen alpha chain
- Finding
- Findings
- full gene sequencing
- Full Mut Anl
- Genetics
- Heredity
- Heritable
- high-throughput sequencing
- HTS
- Inherited
- Molecular pathology
- MOLPATH
- Mut
- Mutations
- Next generation sequencing
- NGS
- Point in time
- Random
- sequencing of entire coding region
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue